Canonical Allele Identifier: PA358827
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 132136
ClinVar RCV Id: RCV000119024 RCV000255214 RCV001136029 RCV001136030 RCV001132648 RCV001132649 RCV001380728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Trp31729Cys
CA358826
NM_001267550.2:c.95187G>C
CA349464189
NM_001267550.2:c.95187G>T