Canonical Allele Identifier: PA2827978171
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1697525
ClinVar RCV Id: RCV002268809
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ile1751Leu
CA16032993
NM_001354899.2:c.5251A>C
CA16032995
NM_001354899.2:c.5251A>T