Canonical Allele Identifier: PA2499230401
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1171161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1661Ile
CA389037201
NM_000257.4:c.4981G>A