Canonical Allele Identifier: PA2828000298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2822243
ClinVar RCV Id: RCV003650976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Cys356Ser
CA16024236
NM_001354902.2:c.1066T>A
CA16024240
NM_001354902.2:c.1067G>C