Canonical Allele Identifier: PA309592
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202560
ClinVar RCV Id: RCV000313900 RCV000329199 RCV000368569 RCV000474657 RCV000273981 RCV000365255 RCV000733449 RCV004539718 RCV003387790
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu10372Gln
CA309590
NM_001267550.2:c.31114G>C