Canonical Allele Identifier: PA185370
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 179894

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Phe252Ser
CA016801
NM_000257.4:c.755T>C