Canonical Allele Identifier: PA141277
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47528
ClinVar RCV Id: RCV000040797 RCV000464223 RCV000726117 RCV002362648
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp30928His
CA141274
NM_001267550.2:c.92782G>C