Canonical Allele Identifier: PA274800
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 191732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met932Thr
CA013102
NM_000257.4:c.2795T>C