Canonical Allele Identifier: PA302611
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192153
ClinVar RCV Id: RCV000172634 RCV000213073 RCV001171262 RCV001086328 RCV002225090 RCV002345598
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Ala23171Gly
CA302610
NM_133378.4:c.69512C>G