Canonical Allele Identifier: PA2827959842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469997

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1783Ile
CA16032962
NM_001354897.2:c.5348C>T