Canonical Allele Identifier: PA658663271
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 454370

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln1267His
CA038976
NM_000257.4:c.3801G>C
CA389042037
NM_000257.4:c.3801G>T