Canonical Allele Identifier: PA916040822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Gln1970Glu
CA16034137
NM_001354896.2:c.5908C>G