Canonical Allele Identifier: PA2828043925
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 422390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Asn1782Ser
CA16033859
NM_001354904.2:c.5345A>G