Canonical Allele Identifier: PA2826429426
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1058369
ClinVar RCV Id: RCV001367501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Ser34196Asn
CA349400228
NM_001256850.1:c.102587G>A