Canonical Allele Identifier: PA2827989940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2560Asn
CA16038277
NM_001354900.2:c.7679G>A