Canonical Allele Identifier: PA645402177
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236643

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser2464Tyr
CA047889
NM_001127510.3:c.7391C>A