Canonical Allele Identifier: PA311861
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203265
ClinVar RCV Id: RCV000468744 RCV001721180
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Tyr5965His
CA311859
NM_001267550.2:c.17893T>C