Canonical Allele Identifier: PA916040383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ile1597Ser
CA16031720
NM_001354896.2:c.4790T>G