Canonical Allele Identifier: PA2827990152
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 838474

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile2625Met
CA16038705
NM_001354900.2:c.7875T>G