Canonical Allele Identifier: PA2827986572
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1331975
ClinVar RCV Id: RCV001804491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1531Ser
CA16031672
NM_001354900.2:c.4592T>G