Canonical Allele Identifier: PA2825112123
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2583135
ClinVar RCV Id: RCV003334423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.His1003Tyr
CA389045922
NM_000257.4:c.3007C>T