Canonical Allele Identifier: PA645414842
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 237432
ClinVar RCV Id: RCV000226286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp382Tyr
CA10583171
NM_000257.4:c.1144G>T