Canonical Allele Identifier: PA2828760974
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503128
ClinVar RCV Id: RCV002022668
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365374.1:p.Ser177Arg
CA350916348
NM_001378445.1:c.531T>G
CA350916350
NM_001378445.1:c.531T>A
CA350916362
NM_001378445.1:c.529A>C