Canonical Allele Identifier: PA915994316
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 724759
ClinVar RCV Id: RCV000898724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro179Ala
CA378920995
NM_005343.4:c.535C>G