Canonical Allele Identifier: PA178932
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 166133
ClinVar RCV Id: RCV000152385 RCV000172372 RCV000242706 RCV000265162 RCV000268918 RCV000320266 RCV000363523 RCV000328537 RCV001085700 RCV001170857
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val9186Ile
CA178930
NM_001256850.1:c.27556G>A