Allele Registry

Canonical Allele Identifier: PA2573170307

Gene: HBB HGNC NCBI

ClinVar RCV:

RCV002238578

ClinVar Variation:

1683259

HGVS (amino-acid)	Matching Registered Transcripts
NP_000509.1:p.Val55Ala	CA379273916 NM_000518.5:c.164T>C