Canonical Allele Identifier: PA2828126579
Gene: MRPS22 HGNC NCBI

Linked Data

ClinVar Variation Id: 3209050
ClinVar RCV Id: RCV004504926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350822.1:p.Leu260Val
CA354763065
NM_001363893.1:c.778C>G