Canonical Allele Identifier: PA645505317
Gene: TRIM44 HGNC NCBI

Linked Data

ClinVar Variation Id: 264710
ClinVar RCV Id: RCV000254593
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060053.2:p.Gly155Arg
CA10588017
NM_017583.6:c.463G>A
CA380399688
NM_017583.6:c.463G>C