Canonical Allele Identifier: PA138949
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46683
ClinVar RCV Id: RCV000039953 RCV000082370 RCV000278937 RCV000275531 RCV000389765 RCV000333001 RCV000367843 RCV001079235 RCV001170083
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala7122Thr
CA138945
NM_001267550.2:c.21364G>A