Canonical Allele Identifier: PA2827964751
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418009

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met441Val
CA027319
NM_001354898.2:c.1321A>G