Canonical Allele Identifier: PA2741817650
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632000
ClinVar RCV Id: RCV003405966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Leu1347Pro
CA5644021
NM_000392.5:c.4040T>C