Canonical Allele Identifier: PA2825108339
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1979840
ClinVar RCV Id: RCV002756167

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Pro30Thr
CA257826921
NM_000257.4:c.88C>A