Canonical Allele Identifier: PA915957424
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 656264

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1453Pro
CA389038932
NM_000257.4:c.4358T>C