Canonical Allele Identifier: PA206707
Gene: TNNI2 HGNC NCBI

Linked Data

ClinVar Variation Id: 212411
ClinVar RCV Id: RCV000193314

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003273.1:p.Lys175Asn
CA206706
NM_003282.4:c.525G>T
CA379106959
NM_003282.4:c.525G>C