Canonical Allele Identifier: PA1139725188
Gene: ARSG HGNC NCBI
ClinVar RCV:
RCV001230639
ClinVar Variation:
957632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_055775.2:p.Gln229His
CA400743329
NM_014960.4:c.687G>C
CA400743330
NM_014960.4:c.687G>T