Canonical Allele Identifier: PA2827959182
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1582Phe
CA039634
NM_001354897.2:c.4744A>T