Canonical Allele Identifier: PA2827942213
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met891Thr
CA10578343
NM_001354895.2:c.2672T>C