Canonical Allele Identifier: PA916065767
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 448799
ClinVar RCV Id: RCV000517781 RCV000617706 RCV000550143 RCV000786258
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_597681.4:p.Lys7047Gln
CA1994992
NM_133437.4:c.21139A>C