Canonical Allele Identifier: PA339422
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216165
ClinVar RCV Id: RCV000564170 RCV003765278 RCV003996976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ile1506Arg
CA339419
NM_001127511.3:c.4517T>G