Canonical Allele Identifier: PA309867
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 180568
ClinVar RCV Id: RCV000157555 RCV000184542 RCV000643915 RCV003137688
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Ala15408Thr
CA309865
NM_001267550.2:c.46222G>A