Canonical Allele Identifier: PA1139675258
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 964036
ClinVar RCV Id: RCV001238173

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1666Glu
CA389037168
NM_000257.4:c.4998C>G
CA389037169
NM_000257.4:c.4998C>A