Canonical Allele Identifier: PA190272
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41501
ClinVar RCV Id: RCV000034383 RCV000164189 RCV000409913 RCV001174835 RCV003315544 RCV003996151
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Glu893Lys
CA007732
NM_000038.6:c.2677G>A