Allele Registry

Canonical Allele Identifier: PA125093

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016544

RCV000641570

ClinVar Variation:

15306

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val24Phe	CA125092 NM_000518.5:c.70G>T