Canonical Allele Identifier: PA2827996230
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ala1696Val
CA041104
NM_001354901.2:c.5087C>T