Canonical Allele Identifier: PA2827986869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asn1626Ser
CA16032272
NM_001354900.2:c.4877A>G