Canonical Allele Identifier: PA286632
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127304
ClinVar RCV Id: RCV000115102 RCV000411965 RCV000766438 RCV003315630 RCV003997222 RCV003743564
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Lys1768Glu
CA010041
NM_000038.6:c.5302A>G