Canonical Allele Identifier: PA180546
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 177633
ClinVar RCV Id: RCV000476946 RCV000853450 RCV000845306 RCV001197200 RCV002255095 RCV001171166 RCV001699043 RCV002321633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Ala114Val
CA004337
NM_000364.3:c.341C>T