Canonical Allele Identifier: PA2827989619
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41514
ClinVar RCV Id: RCV000034399 RCV000077994 RCV000157722 RCV000239067 RCV000307201 RCV001353410 RCV003315545
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2461Ser
CA013731
NM_001354900.2:c.7381G>A