Canonical Allele Identifier: PA891866040
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 45302
ClinVar RCV Id: RCV000038461 RCV000560800 RCV001659973 RCV001813352 RCV004018873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Leu15Pro
CA135982
NM_001318054.2:c.44T>C