Canonical Allele Identifier: PA311159
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_001254479.2:p.Lys34560Arg
CA311157
NM_001267550.2:c.103679A>G