Canonical Allele Identifier: PA2827979816
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ala2258Val
CA012589
NM_001354899.2:c.6773C>T