Canonical Allele Identifier: PA2825644101
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2403Leu
CA047405
NM_001127511.3:c.7208C>T