Allele Registry

Canonical Allele Identifier: PA124660

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016202

ClinVar Variation:

15055

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.His3Arg	CA124659 NM_000519.4:c.8A>G