Canonical Allele Identifier: PA2828016641
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411407
ClinVar RCV Id: RCV001013737 RCV003651856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Ser542Phe
CA16025529
NM_001354903.2:c.1625C>T