Canonical Allele Identifier: PA916040472
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490290
ClinVar RCV Id: RCV000581567 RCV000646350 RCV001764701 RCV003538361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1685Asp
CA040350
NM_001354896.2:c.5053A>G