Canonical Allele Identifier: PA237964
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_596869.4:p.Pro13411Leu
CA237963
NM_133378.4:c.40232C>T