Canonical Allele Identifier: PA2827988237
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470038

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Pro2045Ala
CA044235
NM_001354900.2:c.6133C>G