Allele Registry

Canonical Allele Identifier: PA124685

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016223

ClinVar Variation:

15071

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Arg31Thr	CA124684 NM_000519.4:c.92G>C