Canonical Allele Identifier: PA2828032177
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 925531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser271Thr
CA16023258
NM_001354904.2:c.812G>C