Canonical Allele Identifier: PA2825644298
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2159583
ClinVar RCV Id: RCV003653655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2469Phe
CA048129
NM_001127511.3:c.7406C>T