Canonical Allele Identifier: PA2827973911
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Met438Val
CA027319
NM_001354899.2:c.1312A>G