Canonical Allele Identifier: PA916071774
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12601
ClinVar RCV Id: RCV000013434 RCV000022795 RCV000439343 RCV000587258 RCV000681435 RCV001255683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gln61Lys
CA122547
NM_176795.5:c.181C>A