Canonical Allele Identifier: PA2827982792
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg342Ser
CA004084
NM_001354900.2:c.1026G>T
CA16023939
NM_001354900.2:c.1026G>C