Allele Registry

Canonical Allele Identifier: PA124696

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016231

ClinVar Variation:

15078

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Glu44Gly	CA124695 NM_000519.4:c.131A>G