Canonical Allele Identifier: PA2825021165
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_000029.2:p.Ala1654Gly
CA16032195
NM_000038.6:c.4961C>G