Canonical Allele Identifier: PA2825021385
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2010885
ClinVar RCV Id: RCV003742930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1707Cys
CA16032522
NM_000038.6:c.5120C>G