Canonical Allele Identifier: PA2827990153
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 640552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2625Val
CA16038700
NM_001354900.2:c.7873A>G