Canonical Allele Identifier: PA2825108909
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2506164

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly214Asp
CA389052351
NM_000257.4:c.641G>A