Canonical Allele Identifier: PA2830205717
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 535665
ClinVar RCV Id: RCV000643789 RCV000829330
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Thr21201Ser
CA1990648
NM_133378.4:c.63602C>G
CA1990651
NM_133378.4:c.63601A>T