Canonical Allele Identifier: PA2573165171
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1370753
ClinVar RCV Id: RCV001899417

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1574Pro
CA389037781
NM_000257.4:c.4721G>C