Canonical Allele Identifier: PA2827981142
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 584482
ClinVar RCV Id: RCV000708644
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Asp2656His
CA16038808
NM_001354899.2:c.7966G>C