Canonical Allele Identifier: PA2828013267
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Pro2740Leu
CA050906
NM_001354902.2:c.8219C>T