Canonical Allele Identifier: PA2825362672
Gene: SYCP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 3172583
ClinVar RCV Id: RCV004463506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035364.2:p.Val489Ala
CA134137286
NM_001040274.3:c.1466T>C