Canonical Allele Identifier: PA2828760019
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1503128
ClinVar RCV Id: RCV002022668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365371.1:p.Ser177Arg
CA350916348
NM_001378442.1:c.531T>G
CA350916350
NM_001378442.1:c.531T>A
CA350916362
NM_001378442.1:c.529A>C