Canonical Allele Identifier: PA2825112149
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2175239

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1029Glu
CA389045667
NM_000257.4:c.3085C>G