Canonical Allele Identifier: PA141485
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47602
ClinVar RCV Id: RCV000040871 RCV000457548 RCV000618556 RCV000769105 RCV001130674 RCV001130675 RCV001130677 RCV001293102 RCV001130676 RCV001130678 RCV001703913 RCV004534951
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Asn3026Ile
CA141480
NM_133378.4:c.9077A>T