Canonical Allele Identifier: PA132837
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 43624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Arg94Ser
CA004222
NM_000364.3:c.282A>T
CA344206659
NM_000364.3:c.282A>C