Canonical Allele Identifier: PA141492
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47608
ClinVar RCV Id: RCV000040877 RCV000622118 RCV000525675 RCV000725120 RCV001170525
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val31268Ala
CA141489
NM_001256850.1:c.93803T>C