Allele Registry

Canonical Allele Identifier: PA125065

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016520

ClinVar Variation:

15289

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro37Ser	CA125064 NM_000518.5:c.109C>T