Canonical Allele Identifier: PA2827999942
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482299
ClinVar RCV Id: RCV000575451 RCV001815415 RCV003767137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Gly132Val
CA036174
NM_001354902.2:c.395G>T