Canonical Allele Identifier: PA2827983257
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41520

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile503Thr
CA005403
NM_001354900.2:c.1508T>C