Canonical Allele Identifier: PA913197989
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 594373
ClinVar RCV Id: RCV000729644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Arg910His
CA5643564
NM_000392.5:c.2729G>A