Canonical Allele Identifier: PA658655122
Gene: AIMP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 446035
ClinVar RCV Id: RCV000513934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135887.1:p.Thr104Ala
CA3035682
NM_001142415.2:c.310A>G