Canonical Allele Identifier: PA658804394
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 521789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg54Pro
CA389053702
NM_000257.4:c.161G>C