Canonical Allele Identifier: PA2827956031
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val619Ile
CA006055
NM_001354897.2:c.1855G>A