Canonical Allele Identifier: PA2827966460
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719864

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn992Ser
CA16028012
NM_001354898.2:c.2975A>G