Canonical Allele Identifier: PA2825113870
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2127118
ClinVar RCV Id: RCV003047629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys1930Thr
CA389034480
NM_000257.4:c.5789A>C