Canonical Allele Identifier: PA2827977542
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Arg1561Ser
CA16031778
NM_001354899.2:c.4681C>A