Canonical Allele Identifier: PA2827958848
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala1485Val
CA009538
NM_001354897.2:c.4454C>T