Canonical Allele Identifier: PA310856
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202973
ClinVar RCV Id: RCV000184964 RCV000618251 RCV000697121 RCV000728236 RCV004528966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro28690Ser
CA310855
NM_001256850.1:c.86068C>T