Canonical Allele Identifier: PA645476219
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 402195
ClinVar RCV Id: RCV000454292 RCV002225614 RCV002282147 RCV002522741 RCV003418144 RCV003463833
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064716.2:p.Ser443Pro
CA3916314
NM_020320.5:c.1327T>C