Canonical Allele Identifier: PA2828021826
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411419

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Pro1366Ser
CA038968
NM_001354903.2:c.4096C>T