Allele Registry

Canonical Allele Identifier: PA124706

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016236

ClinVar Variation:

15083

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Arg105Ser	CA124705 NM_000519.4:c.315G>T CA379276706 NM_000519.4:c.315G>C