Canonical Allele Identifier: PA2827998184
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2293Asn
CA16036703
NM_001354901.2:c.6878G>A