Canonical Allele Identifier: PA645412640
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405075
ClinVar RCV Id: RCV000472652 RCV000490792 RCV001250556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Trp34072Arg
CA1985790
NM_001267550.2:c.102214T>C
CA349418116
NM_001267550.2:c.102214T>A