Canonical Allele Identifier: PA2827983516
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140969

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile597Met
CA006359
NM_001354900.2:c.1791A>G