Allele Registry

Canonical Allele Identifier: PA913194628

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000759799

RCV001194401

RCV001835952

ClinVar Variation:

619858

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Ala14Val	CA379274902 NM_000518.5:c.41C>T