Canonical Allele Identifier: PA2825021529
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 801036
ClinVar RCV Id: RCV000985308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Phe1741Cys
CA16032748
NM_000038.6:c.5222T>G