Canonical Allele Identifier: PA2828008910
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1402Met
CA009574
NM_001354902.2:c.4205C>T