Canonical Allele Identifier: PA2827963238
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2820Ser
CA015484
NM_001354897.2:c.8459A>G