Allele Registry

Canonical Allele Identifier: PA124698

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016232

ClinVar Variation:

15079

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.His147Arg	CA124697 NM_000519.4:c.440A>G