Canonical Allele Identifier: PA645412022
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 228165
ClinVar RCV Id: RCV000219688 RCV000535204 RCV001133352 RCV001134820 RCV001133351 RCV001134818 RCV001134819 RCV001311946
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gly30788Ser
CA1987454
NM_001267550.2:c.92362G>A