Canonical Allele Identifier: PA2825641713
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 949271
ClinVar RCV Id: RCV003650743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1632Tyr
CA16032166
NM_001127511.3:c.4894A>T