Canonical Allele Identifier: PA2827979931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 418792
ClinVar RCV Id: RCV000563979 RCV000588074 RCV000686468 RCV004002271 RCV003651920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser2290Gly
CA046510
NM_001354899.2:c.6868A>G