Canonical Allele Identifier: PA176996
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1428Ser
CA014765
NM_000257.4:c.4283T>C