Canonical Allele Identifier: PA2826555307
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 430390
ClinVar RCV Id: RCV000493712

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263276.1:p.Arg139Ser
CA089867
NM_001276347.2:c.415C>A