Canonical Allele Identifier: PA916040962
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142466

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile2101Met
CA011046
NM_001354896.2:c.6303A>G