Canonical Allele Identifier: PA2827966043
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met866Thr
CA10578343
NM_001354898.2:c.2597T>C