Canonical Allele Identifier: PA181797
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178209
ClinVar RCV Id: RCV000154943 RCV000205370 RCV001719966 RCV002415664 RCV004534974
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.His15643Arg
CA181794
NM_001267550.2:c.46928A>G