Canonical Allele Identifier: PA2741817647
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2690803
ClinVar RCV Id: RCV003486349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Ser1342Tyr
CA378127931
NM_000392.5:c.4025C>A