Canonical Allele Identifier: PA645412705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229565
ClinVar RCV Id: RCV000217480 RCV000230688 RCV002223195 RCV002390586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp34478Glu
CA1985604
NM_001267550.2:c.103434C>A
CA349414280
NM_001267550.2:c.103434C>G