Canonical Allele Identifier: PA138832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46640
ClinVar RCV Id: RCV000039910 RCV000464902 RCV001705687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys6220Ser
CA138828
NM_001267550.2:c.18659G>C
CA349560446
NM_001267550.2:c.18658T>A