Canonical Allele Identifier: PA2827986973
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485156
ClinVar RCV Id: RCV000573523 RCV003767216
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1659Thr
CA16032477
NM_001354900.2:c.4975G>A