Canonical Allele Identifier: PA2826403231
Gene: SNAP91 HGNC NCBI

Linked Data

ClinVar Variation Id: 737562
ClinVar RCV Id: RCV000913348
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243646.1:p.Pro614Ser
CA3908187
NM_001256717.2:c.1840C>T