Canonical Allele Identifier: PA098697
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14094

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met349Thr
CA010092
NM_000257.4:c.1046T>C