Canonical Allele Identifier: PA2825644312
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met2473Val
CA048161
NM_001127511.3:c.7417A>G