Canonical Allele Identifier: PA302617
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192154
ClinVar RCV Id: RCV000172635 RCV000249719 RCV000260684 RCV001080773
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp25663Asn
CA302614
NM_001267550.2:c.76987G>A