Canonical Allele Identifier: PA2826554762
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43624
ClinVar RCV Id: RCV000036569 RCV001171168 RCV003450677 RCV003450676 RCV003450675
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001263275.1:p.Arg93Ser
CA004222
NM_001276346.2:c.279A>T
CA344206659
NM_001276346.2:c.279A>C