Canonical Allele Identifier: PA2825113764
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2175452
ClinVar RCV Id: RCV002579234

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Thr1891Ser
CA389034719
NM_000257.4:c.5672C>G
CA389034720
NM_000257.4:c.5671A>T