Canonical Allele Identifier: PA2828678301
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_001363619.1:p.Pro703Ser
CA3908187
NM_001376690.1:c.2107C>T