Canonical Allele Identifier: PA2828000719
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn569Ser
CA16025642
NM_001354902.2:c.1706A>G