Canonical Allele Identifier: PA2827964995
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile519Thr
CA005403
NM_001354898.2:c.1556T>C