Canonical Allele Identifier: PA658655229
Gene: SNRPA HGNC NCBI

Linked Data

ClinVar Variation Id: 446205
ClinVar RCV Id: RCV000515464
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004587.1:p.Phe34Ile
CA405950375
NM_004596.5:c.100T>A