Allele Registry

Canonical Allele Identifier: PA124921

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016389

ClinVar Variation:

15205

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys60Glu	CA124920 NM_000518.5:c.178A>G