Canonical Allele Identifier: PA131981
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43002

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His1419Arg
CA014711
NM_000257.4:c.4256A>G