Canonical Allele Identifier: PA238156
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 192035
ClinVar RCV Id: RCV000172416 RCV000643203
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp4567Glu
CA238155
NM_001267550.2:c.13701T>G
CA349606837
NM_001267550.2:c.13701T>A