Allele Registry

Canonical Allele Identifier: PA127358

Gene: ABO HGNC NCBI

ClinVar RCV:

RCV000019313

ClinVar Variation:

17739

HGVS (amino-acid)	Matching Registered Transcripts
NP_065202.2:p.Pro234Ala	CA127357 NM_020469.3:c.700C>G