Canonical Allele Identifier: PA1139673642
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 881318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys994Arg
CA389046342
NM_000257.4:c.2981A>G