Canonical Allele Identifier: PA2825109806
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg434Ser
CA389050912
NM_000257.4:c.1302G>T
CA389050913
NM_000257.4:c.1302G>C