Canonical Allele Identifier: PA141628
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47658
ClinVar RCV Id: RCV000040927 RCV000619030 RCV000725429 RCV001082764 RCV001135488 RCV001135484 RCV001135485 RCV001135486 RCV001135487 RCV001170292
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr31863Met
CA141626
NM_133378.4:c.95588C>T