Canonical Allele Identifier: PA2825691878
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1691376
ClinVar RCV Id: RCV002254474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg73_Thr74insAsnSerAlaMetArgAspGlnTyrMetArg
CA2573147054
NM_001130442.3:c.191_220dup