Canonical Allele Identifier: PA311237
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203099
ClinVar RCV Id: RCV000261339 RCV000319264 RCV000322851 RCV000376209 RCV000379527 RCV000643648 RCV001704941 RCV002408823
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr35171Ile
CA311235
NM_001267550.2:c.105512C>T