Canonical Allele Identifier: PA2828014168
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186379

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn2650Ser
CA015484
NM_001354905.2:c.7949A>G