Canonical Allele Identifier: PA645383638
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332949
ClinVar RCV Id: RCV000292190 RCV000328902 RCV000332462 RCV000381242 RCV000388836 RCV000678757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg2320Cys
CA2004931
NM_133379.5:c.6958C>T