Canonical Allele Identifier: PA2827986800
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2080400
ClinVar RCV Id: RCV003744845

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Cys1602Ser
CA16032121
NM_001354900.2:c.4804T>A
CA16032124
NM_001354900.2:c.4805G>C