Canonical Allele Identifier: PA2828102665
Gene: SNAP91 HGNC NCBI

Linked Data

ClinVar Variation Id: 737562
ClinVar RCV Id: RCV000913348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350606.1:p.Pro705Ser
CA3908187
NM_001363677.2:c.2113C>T