Canonical Allele Identifier: PA2827986981
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 951569
ClinVar RCV Id: RCV003650768
ClinVar Variation Id: 1745364
ClinVar RCV Id: RCV002336005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gln1660His
CA16032488
NM_001354900.2:c.4980A>C
CA16032489
NM_001354900.2:c.4980A>T