Canonical Allele Identifier: PA2827945146
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Lys1771Arg
CA16032947
NM_001354895.2:c.5312A>G