Canonical Allele Identifier: PA2580139384
Gene: SYCP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2276048
ClinVar RCV Id: RCV004126730
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035364.2:p.Thr188Ile
CA362725999
NM_001040274.3:c.563C>T