ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828680399
Gene: SNAP91
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000913348
ClinVar Variation:
737562
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001363665.1:p.Pro635Ser
CA3908187
NM_001376736.1:c.1903C>T