Canonical Allele Identifier: PA185031
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179736
ClinVar RCV Id: RCV000156534 RCV000643144 RCV002345520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Ser403Thr
CA185027
NM_133379.5:c.1208G>C