Canonical Allele Identifier: PA310997
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203019
ClinVar RCV Id: RCV000327957 RCV000643238 RCV001086209 RCV002362966
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Val32006Met
CA310995
NM_001267550.2:c.96016G>A