Canonical Allele Identifier: PA2742019168
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2763385
ClinVar RCV Id: RCV003515838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Arg41Gln
CA378924802
NM_176795.5:c.122G>A