Canonical Allele Identifier: PA2499230296
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1174884
ClinVar RCV Id: RCV001529162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1925Gly
CA257807342
NM_000257.4:c.5773C>G