Canonical Allele Identifier: PA2827942600
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469855

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Met1014Val
CA16027984
NM_001354895.2:c.3040A>G