Canonical Allele Identifier: PA132036
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1606His
CA015352
NM_000257.4:c.4817G>A