Canonical Allele Identifier: PA658800299
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 537257
ClinVar RCV Id: RCV000646068 RCV004025695
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001430.1:p.Asp98Glu
CA344206497
NM_001001430.3:c.294C>G
CA344206498
NM_001001430.3:c.294C>A