Canonical Allele Identifier: PA2827975035
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg817Cys
CA16026883
NM_001354899.2:c.2449C>T