Canonical Allele Identifier: PA2825505864
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026821
ClinVar RCV Id: RCV001327322

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077074.1:p.Ile59Phe
CA374115066
NM_001083605.3:c.175A>T