Canonical Allele Identifier: PA2825636388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2726739
ClinVar RCV Id: RCV003539003
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1692Ile
CA16032429
NM_001127510.3:c.5075C>T