Canonical Allele Identifier: PA2827989130
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Thr2315Ala
CA046771
NM_001354900.2:c.6943A>G