Canonical Allele Identifier: PA2827987222
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411356

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1729Glu
CA041323
NM_001354900.2:c.5185A>G