Canonical Allele Identifier: PA2825635452
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 957959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met2713Val
CA16039002
NM_001127510.3:c.8137A>G