Canonical Allele Identifier: PA2828018172
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Met790Thr
CA10578343
NM_001354903.2:c.2369T>C