Canonical Allele Identifier: PA2827957704
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1719948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1143Val
CA16028781
NM_001354897.2:c.3428A>T