Canonical Allele Identifier: PA2827965042
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Thr537Met
CA005437
NM_001354898.2:c.1610C>T