Allele Registry

Canonical Allele Identifier: PA124666

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016205

ClinVar Variation:

15058

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Gly26Asp	CA124665 NM_000519.4:c.77G>A