Canonical Allele Identifier: PA2825626631
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2102478
ClinVar RCV Id: RCV003744899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile404Val
CA16023953
NM_001127510.3:c.1210A>G