Canonical Allele Identifier: PA2827981550
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn2782Ser
CA015484
NM_001354899.2:c.8345A>G