Canonical Allele Identifier: PA2825858690
Gene: TCTN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 217696
ClinVar RCV Id: RCV000201680 RCV000310999 RCV000778106
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001137322.1:p.Gly372Arg
CA210299
NM_001143850.3:c.1114G>A
CA387141971
NM_001143850.3:c.1114G>C