Canonical Allele Identifier: PA302829
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 195546
ClinVar RCV Id: RCV000213221 RCV000459255 RCV000724914 RCV001332831 RCV002415758 RCV003486728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg13270Gln
CA302828
NM_133378.4:c.39809G>A