Canonical Allele Identifier: PA354492
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 218010
ClinVar RCV Id: RCV000202147 RCV000569857 RCV000677775 RCV000204603 RCV003534489 RCV003997044 RCV000656743
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asn32Ser
CA051346
NM_000038.6:c.95A>G