Canonical Allele Identifier: PA2825156300
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128025
ClinVar RCV Id: RCV004419928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Arg1289Ser
CA5643978
NM_000392.5:c.3867G>T
CA212867147
NM_000392.5:c.3867G>C