Canonical Allele Identifier: PA2828004804
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485090

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Ile1004Val
CA16028993
NM_001354905.2:c.3010A>G