Canonical Allele Identifier: PA913194071
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 629544
ClinVar RCV Id: RCV000774253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp512Asn
CA389050381
NM_000257.4:c.1534G>A