Canonical Allele Identifier: PA2825640062
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 469920
ClinVar RCV Id: RCV003742679 RCV003338658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Asn1106Ser
CA16028720
NM_001127511.3:c.3317A>G