Canonical Allele Identifier: PA2826977547
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1422549
ClinVar RCV Id: RCV001919589 RCV002344051 RCV003159220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001304983.1:p.Pro100Ser
CA378920992
NM_001318054.2:c.298C>T