Canonical Allele Identifier: PA2830195013
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263732
ClinVar RCV Id: RCV000250405 RCV000868062 RCV001133752 RCV001133754 RCV001133755 RCV001135244 RCV001705387 RCV003114434 RCV004542940 RCV001133753
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg12169Leu
CA1995718
NM_133378.4:c.36506G>T