Allele Registry

Canonical Allele Identifier: PA124668

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016206

ClinVar Variation:

15059

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Gln126Glu	CA124667 NM_000519.4:c.376C>G