Canonical Allele Identifier: PA2827962569
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 236650
ClinVar RCV Id: RCV000227563 RCV000582018 RCV001731536 RCV001559106 RCV003535645 RCV003998693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ala2618Thr
CA10582340
NM_001354897.2:c.7852G>A