Canonical Allele Identifier: PA2825691815
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1478514
ClinVar RCV Id: RCV001974222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asp57_Gln61dup
CA2573147056
NM_001130442.3:c.171_185dup