Canonical Allele Identifier: PA1139675130
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 926457

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1638Lys
CA389037370
NM_000257.4:c.4912G>A