Canonical Allele Identifier: PA2826414009
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46738
ClinVar RCV Id: RCV000040008 RCV000643239 RCV001531338
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Gln7896His
CA139079
NM_001256850.1:c.23688A>C
CA349497838
NM_001256850.1:c.23688A>T