Canonical Allele Identifier: PA302518
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192033
ClinVar RCV Id: RCV000172412 RCV000468843 RCV003987420 RCV003448277
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr4957Pro
CA302515
NM_001267550.2:c.14869A>C