Canonical Allele Identifier: PA2828679829
Gene: SNAP91 HGNC NCBI
ClinVar RCV:
RCV000913348
ClinVar Variation:
737562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001363649.1:p.Pro645Ser
CA3908187
NM_001376720.1:c.1933C>T