Canonical Allele Identifier: PA2829527343
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 957020
ClinVar RCV Id: RCV001229929
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004500.4:p.Glu501Gly
CA350903269
NM_004509.5:c.1502A>G