Canonical Allele Identifier: PA916041588
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433677

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2631Lys
CA16038358
NM_001354896.2:c.7892G>A