Canonical Allele Identifier: PA178654
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 165946
ClinVar RCV Id: RCV000152274 RCV000172300 RCV000306594 RCV000314770 RCV000366954 RCV000621257 RCV000363653 RCV000399359 RCV001170367 RCV001083650 RCV004532696
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg16841His
CA178653
NM_133378.4:c.50522G>A