Canonical Allele Identifier: PA311318
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203122
ClinVar RCV Id: RCV000217473 RCV000643782 RCV002362971 RCV001706159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg1330His
CA311314
NM_133379.5:c.3989G>A