Canonical Allele Identifier: PA2827996286
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1711Glu
CA041323
NM_001354901.2:c.5131A>G