Canonical Allele Identifier: PA2828019750
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 630669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser1025Cys
CA16028731
NM_001354903.2:c.3073A>T