Canonical Allele Identifier: PA658660842
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487059
ClinVar RCV Id: RCV000570752 RCV003459412 RCV003652052 RCV004001210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2626Asn
CA16038448
NM_001127510.3:c.7877C>A