Canonical Allele Identifier: PA2827959393
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231898
ClinVar RCV Id: RCV000213972 RCV000348692 RCV004525836 RCV003650488
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Met1648Thr
CA040178
NM_001354897.2:c.4943T>C