Canonical Allele Identifier: PA2826062661
Gene: NEXN HGNC NCBI

Linked Data

ClinVar Variation Id: 1488557
ClinVar RCV Id: RCV001988645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165780.1:p.Arg410Ser
CA340879318
NM_001172309.2:c.1230G>C
CA340879319
NM_001172309.2:c.1230G>T