Canonical Allele Identifier: PA645383957
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 263726
ClinVar RCV Id: RCV000251789 RCV000541705 RCV001133400 RCV001133396 RCV001133397 RCV001133398 RCV000727950 RCV003479083 RCV004535220 RCV001133399
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Asn3171Ser
CA2004300
NM_133379.5:c.9512A>G