Canonical Allele Identifier: PA2828012392
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_001341831.1:p.Val2501Gly
CA16038224
NM_001354902.2:c.7502T>G