Allele Registry

Canonical Allele Identifier: PA124648

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016195

ClinVar Variation:

15049

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Glu91Val	CA124647 NM_000519.4:c.272A>T