Canonical Allele Identifier: PA1139739283
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 933161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg1607Ser
CA16031778
NM_001354896.2:c.4819C>A