Canonical Allele Identifier: PA183606
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179045
ClinVar RCV Id: RCV000155829 RCV000687436 RCV002225457 RCV002453520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn20664Lys
CA183604
NM_001267550.2:c.61992C>G
CA1992285
NM_001267550.2:c.61992C>A