Allele Registry

Canonical Allele Identifier: PA124681

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016220

ClinVar Variation:

15069

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Val2Ala	CA124680 NM_000519.4:c.5T>C