Canonical Allele Identifier: PA2825641476
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1554Phe
CA039634
NM_001127511.3:c.4660A>T