Canonical Allele Identifier: PA2825112183
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1728462
ClinVar RCV Id: RCV002322665

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1058Gly
CA389045311
NM_000257.4:c.3173A>G