Allele Registry

Canonical Allele Identifier: PA124926

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016395

RCV001811594

RCV003447721

ClinVar Variation:

15208

811500

2664746

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.His93Gln	CA217113620 NM_000518.5:c.279C>G CA217113625 NM_000518.5:c.279C>A