Allele Registry

Canonical Allele Identifier: PA124767

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016275

ClinVar Variation:

15119

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala139Pro	CA124766 NM_000518.5:c.415G>C