Canonical Allele Identifier: PA2825644599
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 926122
ClinVar RCV Id: RCV001188514

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2566Ser
CA16038165
NM_001127511.3:c.7696G>T