Canonical Allele Identifier: PA2826426982
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47617
ClinVar RCV Id: RCV000040886 RCV000226662 RCV000725376 RCV003149663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Arg31504Gln
CA141513
NM_001256850.1:c.94511G>A