Canonical Allele Identifier: PA2827961157
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470052

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2195Asn
CA045325
NM_001354897.2:c.6584G>A