Canonical Allele Identifier: PA2826416814
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 332861
ClinVar RCV Id: RCV000289901 RCV000295707 RCV000324930 RCV000339962 RCV000381963 RCV000554905 RCV000622371 RCV001528437 RCV001798787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg13686Cys
CA1995326
NM_001256850.1:c.41056C>T