Canonical Allele Identifier: PA296684
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1570Glu
CA015247
NM_000257.4:c.4709C>A