Allele Registry

Canonical Allele Identifier: PA124827

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016321

RCV001811149

RCV004526596

ClinVar Variation:

15153

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Asn20Lys	CA124826 NM_000518.5:c.60C>A CA217115328 NM_000518.5:c.60C>G