Canonical Allele Identifier: PA916040467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 655826
ClinVar RCV Id: RCV003536010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Glu1681Asp
CA16032250
NM_001354896.2:c.5043A>C
CA16032251
NM_001354896.2:c.5043A>T