Canonical Allele Identifier: PA2827966832
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1430558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Cys1105Arg
CA16028754
NM_001354898.2:c.3313T>C