Canonical Allele Identifier: PA2828006699
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825134

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1419Ser
CA16031720
NM_001354905.2:c.4256T>G