Canonical Allele Identifier: PA296588
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181212

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1032Asn
CA013351
NM_000257.4:c.3094G>A