Canonical Allele Identifier: PA132147
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43110

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser291Phe
CA016918
NM_000257.4:c.872C>T