Canonical Allele Identifier: PA645411232
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238849
ClinVar RCV Id: RCV000230162 RCV000306715 RCV000266392 RCV000270343 RCV000361378 RCV000376043 RCV000769930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg26981Trp
CA1989275
NM_001267550.2:c.80941C>T