Canonical Allele Identifier: PA2827987384
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231079

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Val1781Gly
CA10578404
NM_001354900.2:c.5342T>G