Canonical Allele Identifier: PA1139697844
Gene: RPS19 HGNC NCBI

Linked Data

ClinVar Variation Id: 894443
ClinVar RCV Id: RCV001135147
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308414.1:p.Pro71Ser
CA406029956
NM_001321485.1:c.211C>T