Canonical Allele Identifier: PA645510122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2352Asn
CA16036703
NM_001127510.3:c.7055G>A