Canonical Allele Identifier: PA2830190864
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332959
ClinVar RCV Id: RCV000274044 RCV000316361 RCV000331363 RCV000366306 RCV000369729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Glu1174Asp
CA2005539
NM_133378.4:c.3522A>C
CA349483110
NM_133378.4:c.3522A>T