Canonical Allele Identifier: PA658814283
Gene: TTN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Asp16261Asn
CA1994743
NM_001267550.2:c.48781G>A