Allele Registry

Canonical Allele Identifier: PA124986

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV000016442

ClinVar Variation:

15240

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Thr85Ile	CA124985 NM_000518.5:c.254C>T