Canonical Allele Identifier: PA2826413264
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_001243779.1:p.Glu6348Asp
CA238120
NM_001256850.1:c.19044A>T
CA349549640
NM_001256850.1:c.19044A>C