Canonical Allele Identifier: PA645410057
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 404896
ClinVar RCV Id: RCV000460440 RCV001560476 RCV004533147 RCV002446775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp16950Glu
CA1994303
NM_001267550.2:c.50850C>A
CA349591784
NM_001267550.2:c.50850C>G