Canonical Allele Identifier: PA2827959527
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1951693
ClinVar RCV Id: RCV003776819

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Phe1694Tyr
CA16032376
NM_001354897.2:c.5081T>A