Canonical Allele Identifier: PA2825111983
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2004162
ClinVar RCV Id: RCV002828190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys940Arg
CA389046941
NM_000257.4:c.2819A>G