Allele Registry

Canonical Allele Identifier: PA125189

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016614

ClinVar Variation:

15363

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Pro37Arg	CA125188 NM_000518.5:c.110C>G