Canonical Allele Identifier: PA215470
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41507
ClinVar RCV Id: RCV000034391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Leu1724Val
CA009899
NM_000038.6:c.5170C>G