Canonical Allele Identifier: PA237625
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191819
ClinVar RCV Id: RCV000172159 RCV000729500 RCV001084327 RCV001133963 RCV001133964 RCV001133965 RCV001133966 RCV001131016 RCV004535168
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34471Gln
CA237623
NM_001267550.2:c.103412G>A