Canonical Allele Identifier: PA311158
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203073
ClinVar RCV Id: RCV000185094 RCV000459723 RCV003486758 RCV003488440
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Lys32919Arg
CA311157
NM_001256850.1:c.98756A>G