Canonical Allele Identifier: PA916052748
Gene: MEIOB HGNC NCBI

Linked Data

ClinVar Variation Id: 440759
ClinVar RCV Id: RCV000508993
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689977.2:p.Asn64Ile
CA394246711
NM_152764.3:c.191A>T