Canonical Allele Identifier: PA141276
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_596869.4:p.Asp28360His
CA141274
NM_133378.4:c.85078G>C