Canonical Allele Identifier: PA2828021401
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133510

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Met1130Val
CA009368
NM_001354906.2:c.3388A>G