Allele Registry

Canonical Allele Identifier: PA144377

Gene: TRIM37 HGNC NCBI

ClinVar RCV:

RCV000049982

RCV003415819

ClinVar Variation:

56569

HGVS (amino-acid)	Matching Registered Transcripts
NP_056109.1:p.Leu76Pro	CA144376 NM_015294.6:c.227T>C