Canonical Allele Identifier: PA237622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191818
ClinVar RCV Id: RCV000172158 RCV000530822 RCV001358750
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Arg34546Cys
CA237620
NM_001267550.2:c.103636C>T