Canonical Allele Identifier: PA645383430
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_001001430.1:p.Lys93Asn
CA10587420
NM_001001430.3:c.279G>T
CA344206561
NM_001001430.3:c.279G>C