Canonical Allele Identifier: PA891863465
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290849

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Gln1357His
CA5644027
NM_000392.5:c.4071G>C
CA378128170
NM_000392.5:c.4071G>T