Canonical Allele Identifier: PA2580138139
Gene: PTCH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449648
ClinVar RCV Id: RCV003171667

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077076.1:p.Ile997Ser
CA374111657
NM_001083607.3:c.2990T>G