Allele Registry

Canonical Allele Identifier: PA124958

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016421

RCV001001409

RCV001272126

RCV001800301

ClinVar Variation:

15224

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys60Asn	CA124957 NM_000518.5:c.180G>C CA217114182 NM_000518.5:c.180G>T