Canonical Allele Identifier: PA2826427093
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 229557
ClinVar RCV Id: RCV000215975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Pro31673Ser
CA1986105
NM_001256850.1:c.95017C>T