Canonical Allele Identifier: PA238122
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192020
ClinVar RCV Id: RCV000172397 RCV001132974 RCV001132973 RCV001132975 RCV001089301 RCV001132971 RCV001132972
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Glu6665Asp
CA238120
NM_001267550.2:c.19995A>T
CA349549640
NM_001267550.2:c.19995A>C