Canonical Allele Identifier: PA2825642051
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2874161
ClinVar RCV Id: RCV003743318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser1740Phe
CA16032859
NM_001127511.3:c.5219C>T