Canonical Allele Identifier: PA2579932182
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 580944
ClinVar RCV Id: RCV000704627
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Cys80Ser
CA378924541
NM_001130442.3:c.239G>C
CA378924550
NM_001130442.3:c.238T>A