Canonical Allele Identifier: PA2580139403
Gene: SYCP2L HGNC NCBI

Linked Data

ClinVar Variation Id: 2350531
ClinVar RCV Id: RCV004196523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035364.2:p.Thr460Ser
CA3634774
NM_001040274.3:c.1379C>G
CA362730807
NM_001040274.3:c.1378A>T