Canonical Allele Identifier: PA2826305699
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_001229722.1:p.Pro675Ser
CA3908187
NM_001242793.2:c.2023C>T