Canonical Allele Identifier: PA2826425348
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 282539
ClinVar RCV Id: RCV000334287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Met28996Leu
CA10604211
NM_001256850.1:c.86986A>T
CA349496003
NM_001256850.1:c.86986A>C