Canonical Allele Identifier: PA2827986790
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg1599Trp
CA009806
NM_001354900.2:c.4795C>T