Canonical Allele Identifier: PA2827974402
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser606Arg
CA10578330
NM_001354899.2:c.1818T>G
CA16025473
NM_001354899.2:c.1816A>C
CA16025479
NM_001354899.2:c.1818T>A