Canonical Allele Identifier: PA191601
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 185312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1746Val
CA009948
NM_001127510.3:c.5236A>G