Canonical Allele Identifier: PA2825153632
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 264318
ClinVar RCV Id: RCV000246459 RCV001854989
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000355.2:p.Lys103Asn
CA10587420
NM_000364.3:c.309G>T
CA344206561
NM_000364.3:c.309G>C