Canonical Allele Identifier: PA139082
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46738
ClinVar RCV Id: RCV000040008 RCV000643239 RCV001531338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Gln8213His
CA139079
NM_001267550.2:c.24639A>C
CA349497838
NM_001267550.2:c.24639A>T