Canonical Allele Identifier: PA2828162091
Gene: ADAR HGNC NCBI

Linked Data

ClinVar Variation Id: 2123252
ClinVar RCV Id: RCV003047275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001351975.1:p.Met586Ile
CA342636791
NM_001365046.1:c.1758G>T
CA342636792
NM_001365046.1:c.1758G>C
CA342636793
NM_001365046.1:c.1758G>A