Canonical Allele Identifier: PA2829435379
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467325
ClinVar RCV Id: RCV000545524
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Arg10715Ser
CA349494156
NM_003319.4:c.32145G>T
CA349494157
NM_003319.4:c.32145G>C