Canonical Allele Identifier: PA2825024822
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760562
ClinVar RCV Id: RCV002409781
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Val2592Gly
CA16038224
NM_000038.6:c.7775T>G