Canonical Allele Identifier: PA658804487
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 520266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp956Glu
CA389046759
NM_000257.4:c.2868T>G
CA389046760
NM_000257.4:c.2868T>A