Canonical Allele Identifier: PA2827950139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2013889
ClinVar RCV Id: RCV003742943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser564Cys
CA16024882
NM_001354896.2:c.1690A>T
CA2580072447
NM_001354896.2:c.1689_1690delinsAT