Canonical Allele Identifier: PA2827944489
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233211

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Asp1570Glu
CA10578381
NM_001354895.2:c.4710T>A
CA16031660
NM_001354895.2:c.4710T>G