Canonical Allele Identifier: PA237965
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 191957
ClinVar RCV Id: RCV000172325 RCV000229401 RCV002415736 RCV002509279
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Pro15979Leu
CA237963
NM_001267550.2:c.47936C>T