Canonical Allele Identifier: PA2573165154
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1395735

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1443His
CA389040086
NM_000257.4:c.4327G>C