Canonical Allele Identifier: PA2827994186
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Pro1081Arg
CA16028829
NM_001354901.2:c.3242C>G