Canonical Allele Identifier: PA2827987163
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1714Val
CA041104
NM_001354900.2:c.5141C>T