Canonical Allele Identifier: PA284288
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47670
ClinVar RCV Id: RCV000040939 RCV000234006 RCV000263000 RCV000252926 RCV000259536 RCV000318171 RCV000372904 RCV000357756 RCV000768827 RCV000852772 RCV001529530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Met32225Leu
CA284286
NM_133378.4:c.96673A>C
CA349411870
NM_133378.4:c.96673A>T