Canonical Allele Identifier: PA103518
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12607
ClinVar RCV Id: RCV000013441 RCV000420974 RCV000432069 RCV000427320 RCV000434059 RCV000438623 RCV000444836
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala146Thr
CA256492
NM_001130442.3:c.436G>A