Canonical Allele Identifier: PA2499230395
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1034575
ClinVar RCV Id: RCV001337317

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr993Ile
CA389046354
NM_000257.4:c.2978C>T