Allele Registry

Canonical Allele Identifier: PA125611

Gene: HBA2 HGNC NCBI

ClinVar RCV:

RCV000016947

RCV001811171

ClinVar Variation:

15661

HGVS (amino-acid)	Matching Registered Transcripts
NP_000508.1:p.His51Asp	CA125610 NM_000517.6:c.151C>G