Canonical Allele Identifier: PA2828095850
Gene: HARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 39620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350465.1:p.Leu130Val
CA343806
NM_001363536.2:c.388C>G