Canonical Allele Identifier: PA296598
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181216
ClinVar RCV Id: RCV000158592

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu1055Met
CA013428
NM_000257.4:c.3163C>A