Canonical Allele Identifier: PA2830213722
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 467156
ClinVar RCV Id: RCV000548147 RCV001130211 RCV001130212 RCV001130213 RCV001130214 RCV001130215 RCV003488678
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597676.3:p.Ser5624Cys
CA1995817
NM_133432.3:c.16871C>G