Canonical Allele Identifier: PA658816746
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 497027
ClinVar RCV Id: RCV000594645 RCV000643852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn31190Lys
CA1987281
NM_001267550.2:c.93570T>A
CA349482231
NM_001267550.2:c.93570T>G