Canonical Allele Identifier: PA309577
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202555
ClinVar RCV Id: RCV000275207 RCV000327843 RCV000345471 RCV000379169 RCV000538876 RCV000384755 RCV000714009 RCV000764339 RCV002282011 RCV001270046 RCV003486747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg9813His
CA309575
NM_001256850.1:c.29438G>A