Canonical Allele Identifier: PA2827974390
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926362

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Leu601Ser
CA16025442
NM_001354899.2:c.1802T>C