Canonical Allele Identifier: PA2825112330
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3074402
ClinVar RCV Id: RCV004013936

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1167Cys
CA037664
NM_000257.4:c.3499C>T