Canonical Allele Identifier: PA311239
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203100
ClinVar RCV Id: RCV000185126 RCV000274755 RCV000271197 RCV000331942 RCV000363562 RCV000328540 RCV000728009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg33611Gln
CA311238
NM_001256850.1:c.100832G>A