Canonical Allele Identifier: PA2828021770
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 230474
ClinVar RCV Id: RCV000214073 RCV003477717 RCV003743650 RCV003997841 RCV000461981
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1358Ser
CA038928
NM_001354903.2:c.4073C>G
CA16030912
NM_001354903.2:c.4072A>T