Canonical Allele Identifier: PA2828019587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 420874

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Arg1004Trp
CA034994
NM_001354903.2:c.3010C>T