Canonical Allele Identifier: PA2828053591
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 919879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn442Ser
CA16025270
NM_001354905.2:c.1325A>G