Allele Registry

Canonical Allele Identifier: PA124662

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016203

ClinVar Variation:

15056

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Gly25Asp	CA124661 NM_000519.4:c.74G>A