Canonical Allele Identifier: PA2827961744
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2367Glu
CA16036732
NM_001354897.2:c.7099A>G