Canonical Allele Identifier: PA2825112245
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1990780
ClinVar RCV Id: RCV002805835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1104Val
CA036711
NM_000257.4:c.3310C>G