Canonical Allele Identifier: PA140991
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47435
ClinVar RCV Id: RCV000040704 RCV000907241 RCV001798185 RCV003137570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr28150His
CA140988
NM_001267550.2:c.84448T>C