Canonical Allele Identifier: PA2828004388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 640552

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile2575Val
CA16038700
NM_001354902.2:c.7723A>G