Canonical Allele Identifier: PA2825641761
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1649Asp
CA040350
NM_001127511.3:c.4945A>G