Canonical Allele Identifier: PA2828007940
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2789833
ClinVar RCV Id: RCV003745773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Pro1618Ser
CA16032989
NM_001354905.2:c.4852C>T