Canonical Allele Identifier: PA891863416
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8412

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Arg768Trp
CA119596
NM_000392.5:c.2302C>T