Canonical Allele Identifier: PA2828000514
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ile453Thr
CA005403
NM_001354902.2:c.1358T>C