Allele Registry

Canonical Allele Identifier: PA099794

Gene: HOXD13 HGNC NCBI

ClinVar RCV:

RCV000016000

RCV003450643

ClinVar Variation:

14872

HGVS (amino-acid)	Matching Registered Transcripts
NP_000514.2:p.Arg306Trp	CA124417 NM_000523.4:c.916C>T