Canonical Allele Identifier: PA1139706744
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 940755
ClinVar RCV Id: RCV001210405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ser189Phe
CA378920852
NM_005343.4:c.566C>T