Canonical Allele Identifier: PA2825023916
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2352Asn
CA16036703
NM_000038.6:c.7055G>A