Canonical Allele Identifier: PA261359
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42948

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1045Leu
CA013375
NM_000257.4:c.3134G>T