Canonical Allele Identifier: PA2828055651
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537440

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn958Ser
CA16028677
NM_001354905.2:c.2873A>G