Canonical Allele Identifier: PA2825644910
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1317229
ClinVar RCV Id: RCV001759101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile2665Ser
CA16038805
NM_001127511.3:c.7994T>G