Canonical Allele Identifier: PA2829601160
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2693094
ClinVar RCV Id: RCV003514672
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Leu171Val
CA378921099
NM_005343.4:c.511C>G