Canonical Allele Identifier: PA2828001644
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg1055Cys
CA035367
NM_001354902.2:c.3163C>T