Canonical Allele Identifier: PA1139675256
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 846989

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1665Asn
CA044655
NM_000257.4:c.4993G>A