Canonical Allele Identifier: PA2499230287
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1013372
ClinVar RCV Id: RCV001871781

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1658Gly
CA389037217
NM_000257.4:c.4973A>G