Canonical Allele Identifier: PA2825156262
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3128018
ClinVar RCV Id: RCV004417851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Trp1200Leu
CA5643860
NM_000392.5:c.3599G>T