Canonical Allele Identifier: PA2827959015
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482319

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1534Val
CA16031338
NM_001354897.2:c.4600A>G