Canonical Allele Identifier: PA181702
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 96307
ClinVar RCV Id: RCV000082433 RCV000154913 RCV000229774 RCV000252341
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ser27083Pro
CA181698
NM_001267550.2:c.81247T>C