Canonical Allele Identifier: PA2580139392
Gene: SYCP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2233123
ClinVar RCV Id: RCV004094137
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035364.2:p.Ile362Leu
CA3634678
NM_001040274.3:c.1084A>T
CA362729950
NM_001040274.3:c.1084A>C