Canonical Allele Identifier: PA2828029001
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 647268
ClinVar RCV Id: RCV002397619 RCV003535922
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ser2297Phe
CA16038139
NM_001354906.2:c.6890C>T