Canonical Allele Identifier: PA2826416383
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404890
ClinVar RCV Id: RCV000619085 RCV000725627 RCV001083684 RCV003150215
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Thr12860Ser
CA1995842
NM_001256850.1:c.38579C>G
CA349650320
NM_001256850.1:c.38578A>T