Canonical Allele Identifier: PA2826410873
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332953
ClinVar RCV Id: RCV000274321 RCV000273247 RCV000334036 RCV000328235 RCV000363172 RCV000730583
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Glu1691Asp
CA2005224
NM_001256850.1:c.5073A>T
CA349456954
NM_001256850.1:c.5073A>C