Canonical Allele Identifier: PA2827959199
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 140839

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Cys1588Gly
CA009712
NM_001354897.2:c.4762T>G