Canonical Allele Identifier: PA2827957638
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val1125Met
CA035105
NM_001354897.2:c.3373G>A