Canonical Allele Identifier: PA2828050070
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn2684Ser
CA015484
NM_001354904.2:c.8051A>G