Canonical Allele Identifier: PA2827980522
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060
ClinVar RCV Id: RCV000565939 RCV003744577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2469Trp
CA16037624
NM_001354899.2:c.7406C>G