Allele Registry

Canonical Allele Identifier: PA124634

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016186

RCV000016187

ClinVar Variation:

15042

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Gly17Arg	CA124633 NM_000519.4:c.49G>C