Canonical Allele Identifier: PA2827977952
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385
ClinVar RCV Id: RCV000572058 RCV000465464 RCV000481145 RCV004001930 RCV002230484
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asn1688Ser
CA040767
NM_001354899.2:c.5063A>G