Canonical Allele Identifier: PA122385
Gene: TNNI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12437
ClinVar RCV Id: RCV000013250 RCV000128668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001139301.1:p.Lys176del
CA122381
NM_001145829.2:c.527_529del
CA379106953
NM_001145829.2:c.523A>T
CA379106962
NM_001145829.2:c.526A>T