Canonical Allele Identifier: PA2830237172
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332767
ClinVar RCV Id: RCV000262505 RCV000265841 RCV000317678 RCV000372563 RCV000375943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Ser17955Arg
CA10611616
NM_133437.4:c.53865C>G
CA349588598
NM_133437.4:c.53865C>A
CA349588607
NM_133437.4:c.53863A>C