Canonical Allele Identifier: PA916041386
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 485089
ClinVar RCV Id: RCV000561196 RCV001284368 RCV004001091 RCV003652029
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2443Asn
CA16037169
NM_001354896.2:c.7328G>A