Canonical Allele Identifier: PA139702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46987
ClinVar RCV Id: RCV000040257 RCV000243472 RCV000312455 RCV000271569 RCV000306752 RCV000407483 RCV000350900 RCV000363806 RCV000755420 RCV000770032 RCV001528376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp13469Asn
CA139699
NM_001256850.1:c.40405G>A