Canonical Allele Identifier: PA2829474618
Gene: NAPA HGNC NCBI

Linked Data

ClinVar Variation Id: 3175115
ClinVar RCV Id: RCV004466444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003818.2:p.His124Arg
CA9540911
NM_003827.4:c.371A>G