Canonical Allele Identifier: PA311129
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 203063
ClinVar RCV Id: RCV000213403 RCV000535734 RCV000725169 RCV002381618
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Cys33836Ser
CA311127
NM_001267550.2:c.101506T>A
CA349420561
NM_001267550.2:c.101507G>C