Canonical Allele Identifier: PA916042443
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn998Ser
CA16028720
NM_001354904.2:c.2993A>G