Allele Registry

Canonical Allele Identifier: PA915965052

Gene: ABCC2 HGNC NCBI

ClinVar RCV:

RCV000988441

RCV002549711

ClinVar Variation:

802627

HGVS (amino-acid)	Matching Registered Transcripts
NP_000383.2:p.Tyr39Phe	CA5642784 NM_000392.5:c.116A>T