Canonical Allele Identifier: PA311185
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203082
ClinVar RCV Id: RCV000458275 RCV000727494 RCV001170287 RCV002399691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33199Gln
CA311184
NM_001256850.1:c.99596G>A