Canonical Allele Identifier: PA181979
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 178269
ClinVar RCV Id: RCV000155010 RCV000172725 RCV000620190 RCV001086015 RCV001133785 RCV001135271 RCV001133784 RCV001133783 RCV001135272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val2772Met
CA181974
NM_133379.5:c.8314G>A