Canonical Allele Identifier: PA2829433138
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_003310.4:p.Thr6701Ser
CA10581867
NM_003319.4:c.20101A>T
CA349618178
NM_003319.4:c.20102C>G