Canonical Allele Identifier: PA658688089
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489474
ClinVar RCV Id: RCV000580121 RCV002529070 RCV003537231
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Pro1992Ser
CA043556
NM_001127510.3:c.5974C>T