Canonical Allele Identifier: PA2828761542
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1491431
ClinVar RCV Id: RCV001986519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365376.1:p.Gly444Arg
CA2154481
NM_001378447.1:c.1330G>A
CA350903323
NM_001378447.1:c.1330G>C