Canonical Allele Identifier: PA2826426233
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 1755861
ClinVar RCV Id: RCV002362169 RCV003138220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Val30318Leu
CA349456531
NM_001256850.1:c.90952G>T
CA349456533
NM_001256850.1:c.90952G>C