Canonical Allele Identifier: PA2827980062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 958591

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2331Ala
CA046787
NM_001354899.2:c.6991T>G