Canonical Allele Identifier: PA2825023939
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1757022
ClinVar RCV Id: RCV002365113

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser2359Leu
CA16036749
NM_000038.6:c.7076C>T