Canonical Allele Identifier: PA2825021170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 825329
ClinVar RCV Id: RCV001023335 RCV003744709
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Thr1655Ile
CA16032201
NM_000038.6:c.4964C>T