Canonical Allele Identifier: PA238469
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192149
ClinVar RCV Id: RCV000172627 RCV000604152 RCV001083852 RCV001129601 RCV001129602 RCV001129603 RCV001129604 RCV001129605 RCV002354445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Pro25983Thr
CA238468
NM_133378.4:c.77947C>A