Canonical Allele Identifier: PA2825633399
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn1667Ser
CA16032272
NM_001127510.3:c.5000A>G