Allele Registry

Canonical Allele Identifier: PA342857

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016566

RCV000589853

RCV001272124

RCV003387731

ClinVar Variation:

15326

36311

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn103Lys	CA342856 NM_000518.5:c.309C>A CA217113423 NM_000518.5:c.309C>G