Canonical Allele Identifier: PA183617
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 179048
ClinVar RCV Id: RCV000155832 RCV000471687 RCV000725815 RCV000618664 RCV001136068 RCV001132677 RCV001132678 RCV001132679 RCV001132680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly15923Arg
CA183614
NM_001267550.2:c.47767G>A
CA349613423
NM_001267550.2:c.47767G>C