Canonical Allele Identifier: PA139664
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46967
ClinVar RCV Id: RCV000040237 RCV000617879 RCV000726234 RCV001087264 RCV001171014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp14473His
CA139661
NM_001267550.2:c.43417G>C