Canonical Allele Identifier: PA2828028993
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1692381

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2295Pro
CA16038121
NM_001354906.2:c.6883T>C