Canonical Allele Identifier: PA2827994092
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411517

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1056Met
CA035105
NM_001354901.2:c.3166G>A