Canonical Allele Identifier: PA645412832
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 405066
ClinVar RCV Id: RCV000474099 RCV002411429 RCV003139639
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001254479.2:p.Phe35214Leu
CA1985226
NM_001267550.2:c.105642C>A
CA349408252
NM_001267550.2:c.105642C>G
CA349408261
NM_001267550.2:c.105640T>C