Canonical Allele Identifier: PA170979
Gene: TGM5 HGNC NCBI

Linked Data

ClinVar Variation Id: 157568
ClinVar RCV Id: RCV000144912
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_963925.2:p.Trp255Arg
CA170978
NM_201631.4:c.763T>C
CA392099406
NM_201631.4:c.763T>A