Canonical Allele Identifier: PA2827995930
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn1608Asp
CA040350
NM_001354901.2:c.4822A>G