Canonical Allele Identifier: PA2828006650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 559952
ClinVar RCV Id: RCV000677752
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Leu1403Val
CA16031609
NM_001354905.2:c.4207C>G