Canonical Allele Identifier: PA658806334
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 507560
ClinVar RCV Id: RCV001132042 RCV001132043 RCV001132044 RCV001132045 RCV001132046 RCV001697352 RCV002331040 RCV003150298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Arg1431Gln
CA2005343
NM_133379.5:c.4292G>A