Allele Registry

Canonical Allele Identifier: PA124652

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016197

ClinVar Variation:

15051

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Glu122Val	CA124651 NM_000519.4:c.365A>T