Canonical Allele Identifier: PA2827986237
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 186197
ClinVar RCV Id: RCV000165744 RCV000210169 RCV000607446 RCV000985303 RCV002516489 RCV003995448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ala1434Val
CA009538
NM_001354900.2:c.4301C>T