Canonical Allele Identifier: PA2825113184
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3071162
ClinVar RCV Id: RCV004014664

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1658Asn
CA389037221
NM_000257.4:c.4972G>A