Canonical Allele Identifier: PA250869
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 83212
ClinVar RCV Id: RCV000074203 RCV000573010 RCV001192945 RCV001854267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ile638Val
CA006325
NM_000038.6:c.1912A>G