Canonical Allele Identifier: PA2826414705
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192000
ClinVar RCV Id: RCV000172370 RCV001130655 RCV001130656 RCV001130657 RCV001130658 RCV001133624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ala9244Thr
CA238069
NM_001256850.1:c.27730G>A