Canonical Allele Identifier: PA645486530
Gene: SYNE2 HGNC NCBI
ClinVar RCV:
RCV000330788
ClinVar Variation:
313567
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_878918.2:p.Gln4051Glu
CA7222029
NM_182914.2:c.12151C>G