Canonical Allele Identifier: PA2827999002
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ser2542Asn
CA16038277
NM_001354901.2:c.7625G>A