Canonical Allele Identifier: PA2828760892
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445889
ClinVar RCV Id: RCV003155808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365374.1:p.Met7Ile
CA350919211
NM_001378445.1:c.21G>T
CA350919214
NM_001378445.1:c.21G>C
CA350919215
NM_001378445.1:c.21G>A