Canonical Allele Identifier: PA891863426
Gene: ABCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 286791
ClinVar RCV Id: RCV000363336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000383.2:p.Arg905Ser
CA5643560
NM_000392.5:c.2715A>T
CA378120817
NM_000392.5:c.2715A>C