Canonical Allele Identifier: PA2829433422
Gene: TTN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp7196Asn
CA1994743
NM_003319.4:c.21586G>A