Canonical Allele Identifier: PA139719
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46995
ClinVar RCV Id: RCV000040265 RCV000304633 RCV000303308 RCV000347554 RCV000358217 RCV000406048 RCV000407706 RCV000727270 RCV001079806 RCV000770026 RCV004541156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Lys12787Asn
CA139717
NM_133378.4:c.38361G>C
CA349629615
NM_133378.4:c.38361G>T