Canonical Allele Identifier: PA141554
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47634
ClinVar RCV Id: RCV000040903 RCV000226035 RCV000620304 RCV001081693 RCV001128954 RCV001131612 RCV001128955 RCV001128953 RCV001131611 RCV001170519
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val31181Met
CA141552
NM_133378.4:c.93541G>A