Canonical Allele Identifier: PA139497
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46910
ClinVar RCV Id: RCV000040180 RCV000154101 RCV000209217 RCV000246075 RCV000271482 RCV000366063 RCV000369218 RCV000402487 RCV000986946 RCV001083564 RCV002227929 RCV004541149 RCV003149645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596870.2:p.Val1034Met
CA139491
NM_133379.5:c.3100G>A