Allele Registry

Canonical Allele Identifier: PA124646

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016193

RCV000016194

ClinVar Variation:

15048

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Ala23Glu	CA124645 NM_000519.4:c.68C>A