Allele Registry

Canonical Allele Identifier: PA124638

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016189

ClinVar Variation:

15044

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Gly137Asp	CA124637 NM_000519.4:c.410G>A