Canonical Allele Identifier: PA2828000299
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ala358Val
CA16024253
NM_001354902.2:c.1073C>T