Canonical Allele Identifier: PA2580498087
Gene: TSSK2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2319552
ClinVar RCV Id: RCV004170169

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443732.3:p.Gly350Arg
CA10096505
NM_053006.5:c.1048G>A
CA410645618
NM_053006.5:c.1048G>C