Canonical Allele Identifier: PA2827955903
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr572Met
CA005437
NM_001354897.2:c.1715C>T