Canonical Allele Identifier: PA915957494
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 638862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1666Asn
CA044679
NM_000257.4:c.4996G>A