Canonical Allele Identifier: PA2828022908
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1744419
ClinVar RCV Id: RCV002342801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Ala1371Gly
CA16032195
NM_001354906.2:c.4112C>G