Canonical Allele Identifier: PA2827995098
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met1354Val
CA009368
NM_001354901.2:c.4060A>G