Canonical Allele Identifier: PA310262
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202779
ClinVar RCV Id: RCV000184710 RCV000460249 RCV001329653 RCV002485246 RCV002453683 RCV003486751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Asp19624Asn
CA310261
NM_001256850.1:c.58870G>A