Canonical Allele Identifier: PA2825638153
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met448Val
CA027319
NM_001127511.3:c.1342A>G