Canonical Allele Identifier: PA1139673842
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 859888
ClinVar RCV Id: RCV001066095

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asp1084Val
CA389044573
NM_000257.4:c.3251A>T