Canonical Allele Identifier: PA2825643896
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537425
ClinVar RCV Id: RCV002360599 RCV003538427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2338Ser
CA16036727
NM_001127511.3:c.7012A>T
CA16036729
NM_001127511.3:c.7013C>G