Canonical Allele Identifier: PA2827965018
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 568451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser527Cys
CA16024927
NM_001354898.2:c.1580C>G