Canonical Allele Identifier: PA2580382327
Gene: GMNN HGNC NCBI

Linked Data

ClinVar Variation Id: 2064210
ClinVar RCV Id: RCV002943295
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056979.1:p.Asn15His
CA3658781
NM_015895.5:c.43A>C