Canonical Allele Identifier: PA645399044
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232811

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met891Thr
CA10578343
NM_001127510.3:c.2672T>C