Canonical Allele Identifier: PA2573165118
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390526
ClinVar RCV Id: RCV001889567

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1159Glu
CA389043771
NM_000257.4:c.3476T>A