Canonical Allele Identifier: PA2827989992
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490366
ClinVar RCV Id: RCV000581808 RCV003538381
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Phe2579Tyr
CA16038409
NM_001354900.2:c.7736T>A