Canonical Allele Identifier: PA2829601170
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1024818
ClinVar RCV Id: RCV001325045 RCV002466661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Pro173Ser
CA378921072
NM_005343.4:c.517C>T