Canonical Allele Identifier: PA2828014957
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_001341835.1:p.His105Arg
CA16023850
NM_001354906.2:c.314A>G