Canonical Allele Identifier: PA2827994895
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Val1293Ala
CA008875
NM_001354901.2:c.3878T>C