Canonical Allele Identifier: PA2829870180
Gene: MYH4 HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060003.2:p.Ala1808Val
CA8388621
NM_017533.2:c.5423C>T