Canonical Allele Identifier: PA2827957823
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1174Val
CA16028993
NM_001354897.2:c.3520A>G