Canonical Allele Identifier: PA2828761340
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011431
ClinVar RCV Id: RCV001309233
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365376.1:p.Met8Thr
CA66763449
NM_001378447.1:c.23T>C