Canonical Allele Identifier: PA2827982249
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 132732
ClinVar RCV Id: RCV000119182 RCV000589003 RCV000579594 RCV003650376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg171His
CA012635
NM_001354900.2:c.512G>A