Allele Registry

Canonical Allele Identifier: PA124690

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016228

ClinVar Variation:

15075

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Glu27Asp	CA124689 NM_000519.4:c.81G>C CA379277196 NM_000519.4:c.81G>T