Canonical Allele Identifier: PA916017165
Gene: HARS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 217508
ClinVar RCV Id: RCV000201520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276022.1:p.Asp61Glu
CA279336
NM_001289093.1:c.183T>G
CA361256011
NM_001289093.1:c.183T>A