Canonical Allele Identifier: PA645400619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229993

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Arg1876Met
CA042448
NM_001127510.3:c.5627G>T