Allele Registry

Canonical Allele Identifier: PA125101

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016550

ClinVar Variation:

15310

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr36Phe	CA125100 NM_000518.5:c.107A>T