Canonical Allele Identifier: PA296666
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181254

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1434Cys
CA014792
NM_000257.4:c.4300C>T