Canonical Allele Identifier: PA2827996287
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 569102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Lys1712Arg
CA16032947
NM_001354901.2:c.5135A>G