Canonical Allele Identifier: PA2827968912
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236616

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ala1730Val
CA041104
NM_001354898.2:c.5189C>T