Canonical Allele Identifier: PA916071679
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 35554
ClinVar RCV Id: RCV000029213 RCV000029212 RCV000032852 RCV000173006 RCV000173005 RCV000422625 RCV000427669 RCV000430227 RCV000437649 RCV000443949 RCV000418725 RCV000420422 RCV000420481 RCV000432361 RCV000439826 RCV000424371 RCV000431824 RCV000419344 RCV000430065 RCV000435072 RCV000439525 RCV000440902 RCV001781319 RCV001813211 RCV001255682 RCV001376004 RCV001849283 RCV003458340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gly13Arg
CA129950
NM_176795.5:c.37G>C