Canonical Allele Identifier: PA2828000675
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 428132

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Arg549Trp
CA16025509
NM_001354902.2:c.1645C>T