Canonical Allele Identifier: PA138677
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46588
ClinVar RCV Id: RCV000039858 RCV000534664 RCV000724172 RCV001132890 RCV001132891 RCV001136315 RCV001136316 RCV001136317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asp3601Asn
CA138675
NM_133378.4:c.10801G>A