Canonical Allele Identifier: PA132125
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43096

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val236Ile
CA016646
NM_000257.4:c.706G>A