Canonical Allele Identifier: PA916005795
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 519034
ClinVar RCV Id: RCV000621438

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263274.1:p.Ala167Ser
CA344204646
NM_001276345.2:c.499G>T