Canonical Allele Identifier: PA143963
Gene: GFM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 55856
ClinVar RCV Id: RCV000049273 RCV000196748 RCV002513673
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_115756.2:p.Asp576Glu
CA143962
NM_032380.5:c.1728T>A
CA360077343
NM_032380.5:c.1728T>G