Canonical Allele Identifier: PA2828029053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41537

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2303Ile
CA014009
NM_001354906.2:c.6908G>T