Allele Registry

Canonical Allele Identifier: PA124725

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016249

RCV000144412

RCV000641406

RCV001811146

ClinVar Variation:

15096

156328

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Lys145Asn	CA124724 NM_000518.5:c.435G>C CA233188 NM_000518.5:c.435G>T