Canonical Allele Identifier: PA2825112114
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3073494
ClinVar RCV Id: RCV004016500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu992Pro
CA389046364
NM_000257.4:c.2975T>C