Canonical Allele Identifier: PA645402214
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Val2499Leu
CA10578444
NM_001127510.3:c.7495G>C