Canonical Allele Identifier: PA2829600757
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1355749
ClinVar RCV Id: RCV001888117
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Ile36Thr
CA216883279
NM_005343.4:c.107T>C