Canonical Allele Identifier: PA2828053880
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ser474Arg
CA10578330
NM_001354905.2:c.1422T>G
CA16025473
NM_001354905.2:c.1420A>C
CA16025479
NM_001354905.2:c.1422T>A