Allele Registry

Canonical Allele Identifier: PA124907

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016381

RCV003236444

RCV003736539

ClinVar Variation:

15198

2506213

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn140Lys	CA124906 NM_000518.5:c.420T>A CA379273655 NM_000518.5:c.420T>G