Canonical Allele Identifier: PA916039650
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127278
ClinVar RCV Id: RCV000115070 RCV000198802 RCV000417366 RCV000679049 RCV001353927 RCV003743561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Val627Ile
CA006055
NM_001354896.2:c.1879G>A