Canonical Allele Identifier: PA2827957695
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1430558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Cys1140Arg
CA16028754
NM_001354897.2:c.3418T>C