Canonical Allele Identifier: PA2825642034
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala1737Val
CA041104
NM_001127511.3:c.5210C>T