Canonical Allele Identifier: PA2826417105
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_001243779.1:p.Lys14279Gln
CA1994992
NM_001256850.1:c.42835A>C