Canonical Allele Identifier: PA2825644619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946681
ClinVar RCV Id: RCV003538615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His2573Arg
CA16038215
NM_001127511.3:c.7718A>G