Canonical Allele Identifier: PA140297
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47197
ClinVar RCV Id: RCV000040467 RCV000082417 RCV000143969 RCV000262231 RCV000297845 RCV000312697 RCV000357132 RCV000393151 RCV000619500 RCV000852825 RCV001086280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ile12257Val
CA140295
NM_133432.3:c.36769A>G