Canonical Allele Identifier: PA2827964661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418008

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala415Thr
CA16024191
NM_001354898.2:c.1243G>A