Canonical Allele Identifier: PA117353
Gene: TRIM37 HGNC NCBI

Linked Data

ClinVar Variation Id: 5246
ClinVar RCV Id: RCV000005558 RCV000729885
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056109.1:p.Ser287Asn
CA117351
NM_015294.6:c.860G>A