Canonical Allele Identifier: PA2827950778
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1035Ser
CA16028012
NM_001354896.2:c.3104A>G