Canonical Allele Identifier: PA2573165178
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1390546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1614Met
CA389037537
NM_000257.4:c.4840G>A