Allele Registry

Canonical Allele Identifier: PA124656

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016199

RCV000016200

ClinVar Variation:

15053

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Asn13Lys	CA124655 NM_000519.4:c.39T>A CA379277276 NM_000519.4:c.39T>G