Canonical Allele Identifier: PA2499230333
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172022
ClinVar RCV Id: RCV001525605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu965Val
CA389046677
NM_000257.4:c.2894A>T