Allele Registry

Canonical Allele Identifier: PA124702

Gene: HBD HGNC NCBI

ClinVar RCV:

RCV000016234

ClinVar Variation:

15081

HGVS (amino-acid)	Matching Registered Transcripts
NP_000510.1:p.Asn58Lys	CA124701 NM_000519.4:c.174C>A CA379276997 NM_000519.4:c.174C>G