Canonical Allele Identifier: PA289091
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46988
ClinVar RCV Id: RCV000040258 RCV000118755 RCV000242768 RCV000770031 RCV001133295 RCV001133296 RCV001133292 RCV001133294 RCV001084207 RCV001133293 RCV004534897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys12568Asn
CA289089
NM_133378.4:c.37704G>T
CA349634733
NM_133378.4:c.37704G>C