Canonical Allele Identifier: PA2828007752
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1586Val
CA009948
NM_001354905.2:c.4756A>G