Canonical Allele Identifier: PA122384
Gene: TNNI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12437

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003273.1:p.Lys176del
CA122381
NM_003282.4:c.527_529del
CA379106953
NM_003282.4:c.523A>T
CA379106962
NM_003282.4:c.526A>T