Canonical Allele Identifier: PA2827964727
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487006

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asp434Gly
CA16024318
NM_001354898.2:c.1301A>G