Canonical Allele Identifier: PA296602
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1058Tyr
CA013452
NM_000257.4:c.3172G>T