Canonical Allele Identifier: PA2827686707
Gene: ARSG HGNC NCBI

Linked Data

ClinVar Variation Id: 957632
ClinVar RCV Id: RCV001230639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339828.1:p.Gln229His
CA400743329
NM_001352899.2:c.687G>C
CA400743330
NM_001352899.2:c.687G>T