Canonical Allele Identifier: PA645472434
Gene: SNAPIN HGNC NCBI

Linked Data

ClinVar Variation Id: 402168
ClinVar RCV Id: RCV000454257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036569.1:p.Arg55Trp
CA16609499
NM_012437.6:c.163C>T