Canonical Allele Identifier: PA2573165175
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1483269
ClinVar RCV Id: RCV001998694

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1598Pro
CA389037623
NM_000257.4:c.4793A>C