Canonical Allele Identifier: PA1139673523
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 834192

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu921Ala
CA034207
NM_000257.4:c.2762A>C