Canonical Allele Identifier: PA16040141
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_000029.2:p.Ala2608Thr
CA10582340
NM_000038.6:c.7822G>A