Canonical Allele Identifier: PA2825112155
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2137559
ClinVar RCV Id: RCV003062620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1038Pro
CA257817954
NM_000257.4:c.3113T>C