Canonical Allele Identifier: PA916060910
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405108
ClinVar RCV Id: RCV000462032 RCV001129211 RCV001129212 RCV001131900 RCV001131901 RCV001129213 RCV001569574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Arg9220Trp
CA1998969
NM_133378.4:c.27658C>T