Canonical Allele Identifier: PA2825643884
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438887

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2334Asn
CA16036703
NM_001127511.3:c.7001G>A