Canonical Allele Identifier: PA311377
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203134
ClinVar RCV Id: RCV000714053 RCV001079944 RCV002345663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Met1822Leu
CA311374
NM_001267550.2:c.5464A>C
CA349451817
NM_001267550.2:c.5464A>T