Allele Registry

Canonical Allele Identifier: PA124694

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016230

ClinVar Variation:

15077

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Cys94Gly	CA124693 NM_000519.4:c.280T>G