Canonical Allele Identifier: PA2828013127
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485117

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2708Pro
CA16039553
NM_001354902.2:c.8122T>C