Canonical Allele Identifier: PA2825635262
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala2608Val
CA16038328
NM_001127510.3:c.7823C>T