Canonical Allele Identifier: PA2827987193
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 627696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Lys1721Thr
CA16032881
NM_001354900.2:c.5162A>C