Canonical Allele Identifier: PA2825639428
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485127

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His895Arg
CA033216
NM_001127511.3:c.2684A>G