Canonical Allele Identifier: PA2827962563
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 860900
ClinVar RCV Id: RCV002240540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2616Ile
CA16038312
NM_001354897.2:c.7846G>A