Canonical Allele Identifier: PA138938
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46676
ClinVar RCV Id: RCV000039946 RCV000172490 RCV001130955 RCV001130956 RCV001130957 RCV000852945 RCV001130954 RCV001085831 RCV001130953 RCV004541136
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala570Val
CA138935
NM_001267550.2:c.1709C>T