Canonical Allele Identifier: PA658800738
Gene: ARSB HGNC NCBI

Linked Data

ClinVar Variation Id: 527327
ClinVar RCV Id: RCV000632185 RCV003128671
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000037.2:p.Thr216Ile
CA3318218
NM_000046.5:c.647C>T