Canonical Allele Identifier: PA2825113067
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714009
ClinVar RCV Id: RCV002296992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser1600Pro
CA389037612
NM_000257.4:c.4798T>C