Canonical Allele Identifier: PA916040391
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 188075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1607Cys
CA009735
NM_001354896.2:c.4819C>T