Canonical Allele Identifier: PA2827980880
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3074632
ClinVar RCV Id: RCV004014166

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2580Val
CA16038328
NM_001354899.2:c.7739C>T