Canonical Allele Identifier: PA2830208029
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 502205
ClinVar RCV Id: RCV000595985 RCV001130883 RCV001130885 RCV001130887 RCV001130884 RCV001130886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr25216Met
CA1988932
NM_133378.4:c.75647C>T