Allele Registry

Canonical Allele Identifier: PA099831

Gene: HOXD13 HGNC NCBI

ClinVar RCV:

RCV000015997

RCV000015998

ClinVar Variation:

14870

HGVS (amino-acid)	Matching Registered Transcripts
NP_000514.2:p.Ser316Cys	CA124416 NM_000523.4:c.947C>G