Allele Registry

Canonical Allele Identifier: PA2826020989

Gene: PALLD HGNC NCBI

ClinVar RCV:

RCV003099319

RCV004049043

ClinVar Variation:

1729210

HGVS (amino-acid)	Matching Registered Transcripts
NP_001159582.1:p.Asp591His	CA3136080 NM_001166110.2:c.1771G>C