Canonical Allele Identifier: PA132133
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg243Cys
CA016694
NM_000257.4:c.727C>T