Canonical Allele Identifier: PA2827990180
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1761670
ClinVar RCV Id: RCV002419243
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2632Ile
CA16038747
NM_001354900.2:c.7895G>T