Canonical Allele Identifier: PA139229
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46799
ClinVar RCV Id: RCV000040069 RCV001131058 RCV001131059 RCV001131061 RCV001131060 RCV001131062 RCV004534881 RCV003128574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn8021His
CA139227
NM_133378.4:c.24061A>C