Allele Registry

Canonical Allele Identifier: PA124683

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016221

RCV000016222

RCV000398301

RCV001107109

RCV003987322

ClinVar Variation:

15070

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Ala28Ser	CA124682 NM_000519.4:c.82G>T