Canonical Allele Identifier: PA2825112803
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2051350
ClinVar RCV Id: RCV002927186

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1453Val
CA389038936
NM_000257.4:c.4357C>G