Canonical Allele Identifier: PA184858
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 179657
ClinVar RCV Id: RCV000156453 RCV003531988
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Asn110Ser
CA004329
NM_000364.3:c.329A>G