Allele Registry

Canonical Allele Identifier: PA124779

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016283

ClinVar Variation:

15125

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Gly75Val	CA124778 NM_000518.5:c.224G>T