Canonical Allele Identifier: PA2825642062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 627696

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys1744Thr
CA16032881
NM_001127511.3:c.5231A>C