Canonical Allele Identifier: PA2499230332
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys918Arg
CA389047175
NM_000257.4:c.2753A>G