Canonical Allele Identifier: PA2827971970
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_001341827.1:p.Asp2659His
CA16038808
NM_001354898.2:c.7975G>C