Canonical Allele Identifier: PA2825641760
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1649Ser
CA16032272
NM_001127511.3:c.4946A>G