Canonical Allele Identifier: PA2828007787
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482513

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Thr1069Ala
CA035507
NM_001354902.2:c.3205A>G