Canonical Allele Identifier: PA2827987137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1705Val
CA009948
NM_001354900.2:c.5113A>G