Canonical Allele Identifier: PA2827996139
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Ile1669Val
CA040889
NM_001354901.2:c.5005A>G