Canonical Allele Identifier: PA2828012835
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Met2622Thr
CA16039005
NM_001354902.2:c.7865T>C