Allele Registry

Canonical Allele Identifier: PA124901

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016378

ClinVar Variation:

15195

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys121Glu	CA124900 NM_000518.5:c.361A>G