Allele Registry

Canonical Allele Identifier: PA124704

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016235

ClinVar Variation:

15082

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Leu89Val	CA124703 NM_000519.4:c.265C>G