Canonical Allele Identifier: PA2573165099
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1462306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1005Glu
CA389045900
NM_000257.4:c.3013C>G