Canonical Allele Identifier: PA2827998350
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn2343Ser
CA047217
NM_001354901.2:c.7028A>G