Canonical Allele Identifier: PA645409917
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238787
ClinVar RCV Id: RCV000231819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Thr15766Ser
CA10581867
NM_001267550.2:c.47296A>T
CA349618178
NM_001267550.2:c.47297C>G