Canonical Allele Identifier: PA2827961762
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2082323
ClinVar RCV Id: RCV003534924
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met2374Val
CA046864
NM_001354897.2:c.7120A>G