Canonical Allele Identifier: PA645412855
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 238697

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asn35348Lys
CA1985172
NM_001267550.2:c.106044C>A
CA349407154
NM_001267550.2:c.106044C>G