Canonical Allele Identifier: PA2828012112
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2406Leu
CA013717
NM_001354902.2:c.7217C>T