Allele Registry

Canonical Allele Identifier: PA124636

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016188

ClinVar Variation:

15043

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Pro52Arg	CA124635 NM_000519.4:c.155C>G