Allele Registry

Canonical Allele Identifier: PA125041

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016500

ClinVar Variation:

15274

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His98Tyr	CA125040 NM_000518.5:c.292C>T