Canonical Allele Identifier: PA347264
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 190406
ClinVar RCV Id: RCV000484676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1591Pro
CA347262
NM_000257.4:c.4772T>C