Canonical Allele Identifier: PA2828028089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser2320Leu
CA047405
NM_001354903.2:c.6959C>T