Canonical Allele Identifier: PA2827961806
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 187494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2387Ser
CA012867
NM_001354897.2:c.7160A>G