Allele Registry

Canonical Allele Identifier: PA125177

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016607

ClinVar Variation:

15357

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val112Ala	CA125176 NM_000518.5:c.335T>C