Canonical Allele Identifier: PA2828055616
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 220743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Asn948Ser
CA035035
NM_001354905.2:c.2843A>G