Canonical Allele Identifier: PA2827982331
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470104

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Asp197Glu
CA16023011
NM_001354900.2:c.591T>A
CA16023012
NM_001354900.2:c.591T>G