Canonical Allele Identifier: PA237697
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191850
ClinVar RCV Id: RCV000172192 RCV000435407 RCV000620023 RCV001083580 RCV001132111 RCV001132113 RCV001133035 RCV001132112 RCV001133036
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr31339Ile
CA237695
NM_001267550.2:c.94016C>T