Canonical Allele Identifier: PA2827991821
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 818459
ClinVar RCV Id: RCV001010061
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.His329Arg
CA16023850
NM_001354901.2:c.986A>G