Canonical Allele Identifier: PA2830359634
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2633786
ClinVar RCV Id: RCV003400256
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Gly60_Arg68dup
CA2695201056
NM_176795.5:c.179_205dup