Allele Registry

Canonical Allele Identifier: PA124804

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016304

ClinVar Variation:

15141

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val61Ala	CA124803 NM_000518.5:c.182T>C