Canonical Allele Identifier: PA2828760241
Gene: SP110 HGNC NCBI

Linked Data

ClinVar Variation Id: 65748
ClinVar RCV Id: RCV000055979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365372.1:p.Ile27Leu
CA345072
NM_001378443.1:c.78_79delinsAT
CA350919014
NM_001378443.1:c.79A>C
CA350919015
NM_001378443.1:c.79A>T