Canonical Allele Identifier: PA916041707
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 82636
ClinVar RCV Id: RCV000073625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Met2731Leu
CA014373
NM_001354896.2:c.8191A>C
CA16039003
NM_001354896.2:c.8191A>T