Canonical Allele Identifier: PA2827950829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2061927
ClinVar RCV Id: RCV003534916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asp1051His
CA16028116
NM_001354896.2:c.3151G>C