Canonical Allele Identifier: PA296799
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ser322Thr
CA017009
NM_000257.4:c.964T>A