Canonical Allele Identifier: PA2825643888
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2334Gly
CA16036702
NM_001127511.3:c.7000A>G