Canonical Allele Identifier: PA2827974422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg612Trp
CA16025509
NM_001354899.2:c.1834C>T