Canonical Allele Identifier: PA2828679829
Gene: SNAP91 HGNC NCBI

Linked Data

ClinVar Variation Id: 737562
ClinVar RCV Id: RCV000913348

Amino-acid Alleles

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