Canonical Allele Identifier: PA16039963
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_000029.2:p.Thr1459Ser
CA038928
NM_000038.6:c.4376C>G
CA16030912
NM_000038.6:c.4375A>T