Canonical Allele Identifier: PA645477303
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 429531
ClinVar RCV Id: RCV000492907 RCV001304587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001013.1:p.Val103Asp
CA406030513
NM_001022.3:c.308T>A