Allele Registry

Canonical Allele Identifier: PA124710

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016239

ClinVar Variation:

15086

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Val134Ala	CA124709 NM_000519.4:c.401T>C