Allele Registry

Canonical Allele Identifier: PA645374711

Gene: HOXD13 HGNC NCBI

ClinVar RCV:

RCV000210953

ClinVar Variation:

225656

HGVS (amino-acid)	Matching Registered Transcripts
NP_000514.2:p.Arg306Gly	CA10576048 NM_000523.4:c.916C>G