Canonical Allele Identifier: PA2827983523
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg599Trp
CA16025509
NM_001354900.2:c.1795C>T