Canonical Allele Identifier: PA098639
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177674

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Lys207Gln
CA016563
NM_000257.4:c.619A>C