Canonical Allele Identifier: PA2741816268
Gene: HOXA13 HGNC NCBI

Linked Data

ClinVar Variation Id: 2983467
ClinVar RCV Id: RCV003848082

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000513.2:p.Ala131_Ala133dup