Canonical Allele Identifier: PA2829847653
Gene: GEMIN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3099345
ClinVar RCV Id: RCV004387691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056536.2:p.Thr601Ser
CA286713682
NM_015721.3:c.1802C>G
CA397506341
NM_015721.3:c.1801A>T