Canonical Allele Identifier: PA2826410818
Gene: TTN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243779.1:p.Leu1590Phe
CA349461520
NM_001256850.1:c.4770G>T
CA349461528
NM_001256850.1:c.4770G>C