Canonical Allele Identifier: PA916041007
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 233045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ala2146Val
CA044469
NM_001354896.2:c.6437C>T