Allele Registry

Canonical Allele Identifier: PA354659

Gene: HOXD13 HGNC NCBI

ClinVar Variation Id: 218457

HGVS (amino-acid)	Matching Registered Transcripts
NP_000514.2:p.Tyr167Cys	CA249106 NM_000523.4:c.500A>G