Allele Registry

Canonical Allele Identifier: PA124893

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016374

ClinVar Variation:

15191

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr39Pro	CA124892 NM_000518.5:c.115A>C