Canonical Allele Identifier: PA2827962763
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 640552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile2676Val
CA16038700
NM_001354897.2:c.8026A>G