Canonical Allele Identifier: PA138830
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_596869.4:p.Cys4976Ser
CA138828
NM_133378.4:c.14927G>C
CA349560446
NM_133378.4:c.14926T>A