Allele Registry

Canonical Allele Identifier: PA1139669015

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV001078303

ClinVar Variation:

869262

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Tyr36Cys	CA379274600 NM_000518.5:c.107A>G