Canonical Allele Identifier: PA310014
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202697
ClinVar RCV Id: RCV000220238 RCV000243770 RCV000346465 RCV000306260 RCV000349767 RCV000394740 RCV000405647 RCV000460845 RCV001704907
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg15620Gln
CA310013
NM_001256850.1:c.46859G>A