Canonical Allele Identifier: PA2825638383
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2013889
ClinVar RCV Id: RCV003742943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser528Cys
CA16024882
NM_001127511.3:c.1582A>T
CA2580072447
NM_001127511.3:c.1581_1582delinsAT