Canonical Allele Identifier: PA177035
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 164361

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met528Ile
CA011008
NM_000257.4:c.1584G>A
CA389050257
NM_000257.4:c.1584G>T
CA389050258
NM_000257.4:c.1584G>C