Canonical Allele Identifier: PA2827971348
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2472Thr
CA16037620
NM_001354898.2:c.7414T>A