Canonical Allele Identifier: PA915956691
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 636965
ClinVar RCV Id: RCV000788941

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val420Met
CA389051001
NM_000257.4:c.1258G>A