Canonical Allele Identifier: PA174885
Gene: TRIML1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161839
ClinVar RCV Id: RCV000149375
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_848651.2:p.Lys396Asn
CA174884
NM_178556.5:c.1188A>T
CA358985207
NM_178556.5:c.1188A>C