Canonical Allele Identifier: PA2499230288
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 79511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1659Asn
CA044566
NM_000257.4:c.4975G>A