Canonical Allele Identifier: PA2827977492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482393

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1544Phe
CA039634
NM_001354899.2:c.4630A>T