Canonical Allele Identifier: PA2828023067
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 232583
ClinVar RCV Id: RCV000222795 RCV003765428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341832.1:p.Thr1546Ser
CA10578386
NM_001354903.2:c.4636A>T