Canonical Allele Identifier: PA2579931719
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1347756
ClinVar RCV Id: RCV002050671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Leu159Ser
CA378921182
NM_001130442.3:c.476T>C