Canonical Allele Identifier: PA296594
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 155814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1053Gln
CA013417
NM_000257.4:c.3158G>A