Canonical Allele Identifier: PA296738
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly10Ala
CA013294
NM_000257.4:c.29G>C