Canonical Allele Identifier: PA112461
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 5245
ClinVar RCV Id: RCV000005557
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005207.1:p.Cys109Ser
CA117350
NM_001005207.4:c.326G>C
CA400393228
NM_001005207.4:c.325T>A