Canonical Allele Identifier: PA645510048
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 439412
ClinVar RCV Id: RCV000507769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile646Arg
CA16025550
NM_001127510.3:c.1937T>G