Canonical Allele Identifier: PA645431477
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 281137
ClinVar RCV Id: RCV000350888 RCV000354466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056109.1:p.Arg640His
CA8678175
NM_015294.6:c.1919G>A