Canonical Allele Identifier: PA913198017
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 598357
ClinVar RCV Id: RCV000734730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Leu1347Phe
CA5644020
NM_000392.5:c.4039C>T