Canonical Allele Identifier: PA302385
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191812
ClinVar RCV Id: RCV000172152 RCV000286045 RCV000534990 RCV000619680 RCV001353379
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33402His
CA302383
NM_001256850.1:c.100205G>A