Canonical Allele Identifier: PA2827968660
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Gly1657Ser
CA16032360
NM_001354898.2:c.4969G>A