Allele Registry

Canonical Allele Identifier: PA124658

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016201

ClinVar Variation:

15054

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Val21Glu	CA124657 NM_000519.4:c.62T>A