Canonical Allele Identifier: PA2827957741
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411461

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn1152Thr
CA035313
NM_001354897.2:c.3455A>C