Canonical Allele Identifier: PA645416660
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 228907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met1046Ile
CA035844
NM_000257.4:c.3138G>A
CA389045412
NM_000257.4:c.3138G>T
CA389045413
NM_000257.4:c.3138G>C