Canonical Allele Identifier: PA2827959686
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1042148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1738Val
CA040889
NM_001354897.2:c.5212A>G