Canonical Allele Identifier: PA2827950773
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1034Val
CA16028005
NM_001354896.2:c.3101A>T