Canonical Allele Identifier: PA2825024883
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ala2608Val
CA16038328
NM_000038.6:c.7823C>T