Canonical Allele Identifier: PA2825644817
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761409
ClinVar RCV Id: RCV002416908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Glu2637Gly
CA16038626
NM_001127511.3:c.7910A>G