Canonical Allele Identifier: PA164252
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141021

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gln1746Glu
CA010025
NM_001127511.3:c.5236C>G