Canonical Allele Identifier: PA310661
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 202909
ClinVar RCV Id: RCV000223209 RCV000463691 RCV001535416 RCV002345658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn27253Ser
CA310659
NM_001267550.2:c.81758A>G