Canonical Allele Identifier: PA212699
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43085
ClinVar RCV Id: RCV000035980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1909Pro
CA016422
NM_000257.4:c.5726G>C