Canonical Allele Identifier: PA2829600840
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1954526
ClinVar RCV Id: RCV002705677
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Glu63Asp
CA378924662
NM_005343.4:c.189G>T
CA378924663
NM_005343.4:c.189G>C